ENST00000643794.1:c.-2A>G
|
ENSP00000495765.1:n.-2A>G
|
|
ENST00000651669.1:c.-2A>G
MANE Select
|
ENSP00000499044.1:n.-2A>G
|
|
ENST00000368567.4:c.-2A>G
|
ENSP00000357555.4:n.-2A>G
|
|
ENST00000392558.4:c.-2A>G
|
ENSP00000376341.4:n.-2A>G
|
|
ENST00000477151.1:n.33A>G
|
|
|
ENST00000493224.5:n.33A>G
|
|
|
NM_001030.4:c.-2A>G
|
NP_001021.1:n.-2A>G
|
|
NM_001030.6:c.-2A>G
MANE Select
|
NP_001021.1:n.-2A>G
|
|
NM_001349946.1:c.-219A>G
|
NP_001336875.1:n.-219A>G
|
|
NM_001349947.1:c.-330A>G
|
NP_001336876.1:n.-330A>G
|
|
NM_001349946.2:c.-219A>G
|
NP_001336875.1:n.-219A>G
|
|
NM_001349947.2:c.-330A>G
|
NP_001336876.1:n.-330A>G
|
|